{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "OLC",
      "openfda": {
        "k_number": [
          "K170364",
          "K242302",
          "K082079"
        ],
        "registration_number": [
          "3003300673",
          "3013820501",
          "3027448274",
          "2245304",
          "2936485",
          "2249852"
        ],
        "fei_number": [
          "3003300673",
          "3013820501",
          "3027448274",
          "2245304",
          "3008817245",
          "2936485"
        ]
      },
      "review_panel": "OR",
      "medical_specialty": "SU",
      "device_name": "Scaffold, Partial Medial Meniscal Defects Extending Into The Red/White Zone, Resorbable Bovine Collagen",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General, Plastic Surgery",
      "device_class": "2",
      "definition": "Intended for use in surgical procedures for the repair and reinforcement of soft tissue injuries of the medial meniscus.  In repairing and reinforcing medial meniscal defects, the patient must have an intact meniscal rim and anterior and posterior horns for attachment of the mesh.  In addition, the surgically prepared site must extend at least into the red/white zone of the meniscus to provide sufficient vascularization.    The device reinforces soft tissue and provides a resorbable scaffold that is replaced by the patients own soft tissue.  The device is not a prosthetic device and is not intended to replace normal body structure.",
      "regulation_number": "878.3300",
      "implant_flag": "Y",
      "submission_type_id": "1"
    }
  ]
}